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Merck
CN

SML3733

BAY-0069

≥98% (HPLC)

Synonym(s):

2-Bromo-N-[2-(4-ethylphenyl)-1,3-benzoxazol-5-yl]-5-nitrobenzamide, BAY 0069, BAY0069

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About This Item

Empirical Formula (Hill Notation):
C22H16BrN3O4
CAS Number:
Molecular Weight:
466.28
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality level:
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assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

BAY-0069 is a potent and selective covalent PPARγ inverse agonist (IC50 = 0.22 nM, max inhibition = 88% by cell-based reporter assays) that induces interactions between the PPARγ ligand-binding domain (LBD) and the corepressor NCOR2 (EC50 = 9.6 nM, Emax = 620% by TR-FRET). BAY-0069 exhibits anti-proliferation efficacy against PPARγ-dependent growth in cultures (UM-UC9 IC50 = 2.5 nM, max inhibition = 72%).
Potent and selective covalent PPARγ inverse agonist with anti-proliferation efficacy against PPARγ-dependent growth in cultures.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Discovery and Structure-Based Design of Potent Covalent PPAR? Inverse-Agonists BAY-4931 and BAY-0069
Journal of medicinal chemistry, 65(21), 14843-14863 (2022)

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